Mitoxantrone Injection inactive ingredients by manufacturer
Wondering whether your Mitoxantrone Injection has lactose, gluten, soy, a dye or gelatin in it? The medicine is the same, but the fillers, coatings and colors differ from one company to the next. This page shows what each Mitoxantrone Injection product's FDA label lists, so you can find a version that leaves out what you avoid and ask your pharmacist for it by its NDC.
We have read the FDA labels of 4 of the 4 current Mitoxantrone Injection products on the market today, from 3 companies listing it with the FDA, and lined them up side by side.
Ask about your bottle
Is there something in your Mitoxantrone Injection? Ask in plain words.
Name the company, strength or the NDC on your bottle and the ingredient you avoid. The answer comes only from the FDA labels on this page.
Answers are drawn from the FDA label data on this page and checked against it. They are not medical advice: confirm with your pharmacist before relying on them.
The short answer
Which Mitoxantrone Injection products list lactose, a gluten source, soy, dyes or gelatin?
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LactoseNo checked product
No checked Mitoxantrone Injection product lists lactose.
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Wheat or gluten sourceNo checked product
No checked Mitoxantrone Injection product lists a wheat or gluten source.
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SoyNo checked product
No checked Mitoxantrone Injection product lists soy.
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Synthetic dyesNo checked product
No checked Mitoxantrone Injection product lists synthetic dyes.
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GelatinNo checked product
No checked Mitoxantrone Injection product lists gelatin.
Also listed by some products: Sulfites 1 of 4
Find a version without it
Every current Mitoxantrone Injection product and what its label lists
| Product | Lists | Inactive ingredients on the label |
|---|---|---|
| Fresenius Kabi USA, LLC 1 product | ||
| 2 mg/mL injectionNDC 63323-0132-10 | None of these listed |
Show 3 ingredientsACETIC ACID, SODIUM ACETATE, SODIUM CHLORIDE |
| Hospira, Inc. 1 product | ||
| 2 mg/mL injectionNDC 61703-0343-18 | Sulfites |
Show 5 ingredientsACETIC ACID, SODIUM ACETATE, SODIUM CHLORIDE, SODIUM METABISULFITE, WATER |
| Meitheal Pharmaceuticals Inc. 2 products | ||
| 2 mg/mL injectionNDC 71288-0178-10 | None of these listed |
Show 4 ingredientsACETIC ACID, SODIUM ACETATE ANHYDROUS, SODIUM CHLORIDE, WATER |
| 2 mg/mL injectionNDC 71288-0179-13 | None of these listed |
Show 4 ingredientsACETIC ACID, SODIUM ACETATE ANHYDROUS, SODIUM CHLORIDE, WATER |
A product with none of these listed is not certified to be without them: the label says what the manufacturer declared, and the source of a starch or a flavor is often not stated. The companies are the FDA's labelers, which include repackagers and distributors selling another company's product under their own label. The NDC opens the product's own page, with the full label and its inactive-ingredient notes.
Mitoxantrone Injection without sulfites
Sulfites: metabisulfite or bisulfite preservatives; a concern with sulfite sensitivity or asthma. 1 of 4 checked products list sulfites; 3 do not.
Does not list sulfites
- Fresenius Kabi: 2 mg/mL injection
- Meitheal: 2 mg/mL injection (NDC 71288-0178-10), 2 mg/mL injection (NDC 71288-0179-13)
Lists sulfites
- Hospira: 2 mg/mL injection
At the pharmacy counter
How to use this at the pharmacy counter
- Pick the company whose list suits you and copy the NDC from the table. Many pharmacies order from wholesalers that carry several companies' versions and can request a particular one if you ask before the prescription is filled; some buy from one contracted source only, and a few insurance plans cover only certain NDCs, so ask the pharmacist to check.
- Treat "does not list" as exactly that. The label is what the manufacturer declared; a flavor or a starch may have an unstated source, and lines change. For celiac disease or a serious allergy, ask the manufacturer's medical information line for a written statement about the lot you have.
- Check the bottle each refill. A different company usually means a different shape, color and inactive-ingredient list; the pharmacist can tell you who made it, and the two-NDC comparison shows the difference line by line.
- If you need one company's version kept constant, ask your prescriber to write that company or the NDC on the prescription and tell the pharmacy you need it held. Rules vary by state and plan, so confirm with the pharmacist.
Common questions about Mitoxantrone Injection inactive ingredients
Is Mitoxantrone Injection gluten-free?
Does Mitoxantrone Injection contain lactose?
Does Mitoxantrone Injection contain soy?
Is there a dye-free Mitoxantrone Injection?
Does Mitoxantrone Injection contain gelatin?
Why do the inactive ingredients differ between manufacturers?
Can my pharmacy give me a specific manufacturer's version?
How current is this list?
Sources: the products are the finished Mitoxantrone Injection products in the FDA's current NDC directory (openFDA), as of October 5, 2026; each inactive-ingredient list is the manufacturer's FDA Structured Product Label via DailyMed, as our label sync last read it. The concern groups are HelloPharmacist's classification of the names the label declares. Educational information only, not medical advice; confirm with your pharmacist before relying on a list. ← Back to the Mitoxantrone Injection guide